Silicon appears to be an essential element for proper endochondral ossification and glycosaminoglycan synthesis. Osteochondrosis (OC) is characterized by disturbed endochondral ossification, and glycosaminoglycan loss has been reported in OC lesions. Therefore, silicon may be effective in reducing OC lesions. The objective of the study was to evaluate the effects of supplemental silicon on OC lesion size. Initial radiographs were taken on 2-year-old Standardbreds (n = 44) on private facilities to identify OC defects in the distal third metacarpus/tarsus or osteochondral fragments at the dorsal aspect of the joint and defects/fragments at the distal tibia and on the trochlear ridges of the talus. Only clinically sound horses were included. Follow-up radiographs were taken at 120 days. Radiographs were digitized and the length and height of the OC defects/fragments were measured. Horses meeting study-inclusion requirements (n = 8) were pair-matched by facility and affected joint(s) and assigned to a group: control (receiving 200 g whole grain flour) and silicon supplemented (receiving 200 g bioavailable silicon source). Treatments were top-dressed on the feed for 120 days. Due to the onset of lameness, four horses did not complete the 120-day study duration. There was no effect (P>0.22) of treatment, time or treatment × time on lesion length, height or area. Silicon supplementation did not alter the radiographic appearance of OC lesions. Future research should focus on the effects of a silicon supplement on the prevention of OC lesions.

Kinematic studies of western pleasure horses are limited and were performed before current changes in the stock breed association judging standards on the western pleasure gaits. The objective was to measure the kinematics of the jog and lope of the stock breed western pleasure horse. Reflective markers attached along palpation points of the joint centres of the left forelimb and hind limb of four stock breed western pleasure horses were tracked for five strides for each gait for each horse. Both the jog and lope were determined to be four-beat stepping gaits. During the jogging stance, the elbow (159.7 ± 6.6°), carpal (179.9 ± 1.1°), fore (227.6 ± 2.7°) and hind fetlocks (227.4 ± 6.9°), stifle (159.5 ± 6.5°) and tarsal (166.5 ± 6.5°) joints demonstrated peak extension. The same joints demonstrated during swing peak flexion with the hind fetlock joint having double peaks of flexion (195.7 ± 3.2°, 182.3 ± 2.1°). During loping stance, the elbow (153.4 ± 4.2°), carpal (179.7+0.4°), and fore (228.3 ± 9.7°, 229.8 ± 10.0°) and hind fetlock (232.1 ± 2.6°) joints of the leading limbs demonstrated peak extension with tarsal peak extension (157.0 ± 9.6°) occurring at lift-off. Peak flexion occurred during swing for the elbow (105.1 ± 3.1°), carpus (119.8 ± 6.1°), hip (83.5 ± 5.4°), stifle (129.8 ± 9.6°) and tarsus (127.5 ± 6.1°). Kinematic measurements will assist in objectively defining the stock breed western pleasure gaits.

Twelve mature and six 2-year-old Arabian horses were used to determine the effect of dietary long-chain polyunsaturated omega-3 fatty acid supplementation on plasma fatty acids and lameness. Lameness scores and stride lengths were measured on day 0. Horses were striated and pair-matched according to age, gender, stride length and, for mature horses, lameness score, and each horse was fed either a treatment diet containing 5.95 g of stabilized omega-3 fatty acids plus a fat carrier (FA), for a total of 19.4 g fat, or a control diet containing 49 g of corn oil (CO) for 75 days. Horses were exercised 5 d week− 1, and blood samples were drawn and body weights recorded on days 0, 25, 50 and 75. Lameness scores and stride lengths were recorded again on day 75. Total plasma omega-3 fatty acid concentrations were higher on all days in FA horses than in CO horses. Total plasma omega-6 fatty acids increased from days 0 to 25, remained elevated through day 50 and returned to baseline on day 75 in all horses. The ratio of plasma omega-6:omega-3 fatty acids was lower in FA horses. Horses on FA had increased plasma docosahexaenoic acid (DHA) on days 25, 50 and 75. No difference in walk stride length was noted; however, FA horses tended to have a longer trot stride after supplementation when compared with CO horses. No differences were seen in prostaglandin E2 (PGE2) metabolite or tumour necrosis factor-α as measured in blood serum. In summary, supplementing omega-3 fatty acids increases plasma DHA, although there was no overall increase in omega-3 in FA horses. While a trend to increase trot stride length was seen, no differences in lameness scores between treatments were noted.

This study examined the changing levels of air pollution at major racetracks in the United States over the past 35 years of Grade I Stakes Thoroughbred racing (n = 675) to evaluate the impact on race performance. Information on winning race times, race speed, temperature, track conditions, ozone and particulate matter was analysed using multiple regression and ANOVA. The 8, 9 and 12 furlong races showed slight improvement in winning times over the 35-year time span. Although there was no significant difference in mean race speed in terms of particulate matter (F4,112 = 0.514, α < 0.05), the few races run under ‘hazardous’ ozone levels, based on the Pollutants Standards Index, were markedly slower (F4,251 = 12.365, α < 0.05). A multiple regression analysis of six additional pollutants in the Californian races revealed no significant effects beyond a slight improvement in the 7 furlong races, with decreased nitrogen dioxide levels. Of the nine racetracks with 9 furlong races, winning times in Pimlico and Belmont were approximately 4 s slower than average. Belmont also had the greatest percentage of races with hazardous ozone conditions. Other correlations between year, pollutants and improvements in race time were of small magnitude and may be an artefact of the sample size rather than of true predictive value. While racing under high levels of certain pollutants appears detrimental to equine athletes, very few races are run under these conditions and other factors such as breeding, training and individual variation may play a more significant role than this study could document with respect to pollution.

Five previously untrained yearling sled dogs were evaluated for endurance training-induced changes in maximum oxygen consumption (VO2max) and submaximal blood lactate concentrations. Following 3 weeks of light training followed by 4 weeks of moderate training, VO2max increased by 10%, from 180.2 ± 9.9 to 198.7 ± 19.2 ml kg min− 1 (P = 0.046). Light training was not associated with any increase in VO2max. Blood lactate concentrations at the same absolute intensity decreased by 215%, from 9.2 ± 4.7 to 4.3 ± 2.4 mmol l− 1 (P = 0.022). Speeds associated with oxygen consumptions of 70% VO2max increased by 12%, from 4.8 ± 0.4 to 5.4 ± 0.5 m s− 1 (P = 0.008) and speeds associated with VO2max increased by 21%, from 6.7 ± 0.3 to 8.2 ± 0.7 m s− 1 (P = 0.012).

Muscle function depends in part on the interplay between its activity and its length within the stretch-shortening cycle. The longissimus dorsi is a large epaxial muscle running along the thoracic and lumbar regions of the equine back. Due to its anatomical positioning, the longissimus dorsi has the capability of contributing to many functions: developing bending moments in the dorsoventral and lateral (coupled to axial rotation) directions and also providing stiffness to limit motion in these directions. We hypothesize that the exact function of the longissimus dorsi will vary along the back and between gaits as the relation between activity and motion of the back changes. Electromyograms (EMG) were recorded at walk (inclined and level) and trot (on the level) on a treadmill from the longissimus dorsi at muscle segments T14, T16, T18 and L2. Back motion was additionally measured using a fibre-optic goniometer. Co-contractions of the muscle between its left and right sides were quantified using correlation analysis. A greater dominance of unilateral activity was found at more cranial segments and for level walking, suggesting a greater role of the longissimus dorsi in developing lateral bending moments. Timing of the EMG varied between muscle segments relative to the gait cycle, the locomotor condition tested and the flexion–extension cycle of the back. This supports the hypothesis that the function of the longissimus dorsi changes along the back and between gaits.